A retrospective review of streptococcal infections in pediatric atopic dermatitis.

Abstract:

:In order to assess the clinical characteristics and impact of group A streptococcal infection in children with atopic dermatitis, a retrospective review was performed in children diagnosed with atopic dermatitis who had a skin culture. Culture results and clinical characteristics of those with group A streptococcus were compared with those with Staphlococcus aureus. Infection with group A streptococcus was present in 16%; infection with Staphlococcus aureus was present in 72%, and 14% had mixed cultures. Patients infected with group A streptococcus were more likely to be febrile, to have facial and periorbital involvement, and to be hospitalized compared with those infected with Staphlococcus aureus alone (p ≤ 0.01 for all comparisons). Bacteremia and cellulitis were significantly more common in those infected with group A streptococcus than in those infected with Staphlococcus aureus. Retrospective design and review of only those patients receiving bacterial cultures may select for greater severity than in the general atopic dermatitis population. Group A streptococcus appears to be a significant skin pathogen infecting children with atopic dermatitis. Children with atopic dermatitis and group A streptococcal infection are more likely to have invasive disease and complications than those infected with Staphlococcus aureus alone.

journal_name

Pediatr Dermatol

journal_title

Pediatric dermatology

authors

Sugarman JL,Hersh AL,Okamura T,Howard R,Frieden IJ

doi

10.1111/j.1525-1470.2010.01377.x

subject

Has Abstract

pub_date

2011-05-01 00:00:00

pages

230-4

issue

3

eissn

0736-8046

issn

1525-1470

journal_volume

28

pub_type

杂志文章,多中心研究
  • Complementary and alternative therapy for pediatric acne: A review of botanical extracts, dietary interventions, and oral supplements.

    abstract::Many supplements and products containing botanical extracts are marketed to patients for the treatment of acne vulgaris. Additionally, increasing attention has been paid to the role of diet in acne vulgaris. Studies on this topic including pediatric patients are limited, with variable efficacy data. Despite these limi...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.13904

    authors: Gurnee EA,Kamath S,Kruse L

    更新日期:2019-09-01 00:00:00

  • Generalized lupus panniculitis and antiphospholipid syndrome in a patient without complement deficiency.

    abstract::Generalized chronic cutaneous lupus including lupus panniculitis in childhood is rare and usually occurs in the setting of genetic complement deficiencies. The association with antiphospholipid syndrome is even more rare. We report a 13-year-old girl with extensive lupus panniculitis since the age of 8 months and no e...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.1999.00060.x

    authors: Nousari HC,Kimyai-Asadi A,Santana HM,Diglio GM,Tausk FA,Cohen BA

    更新日期:1999-07-01 00:00:00

  • Skin cancer prevention counseling and clinical practices of pediatricians.

    abstract::Little is known about pediatricians' counseling and clinical practices to reduce skin cancer risk among their patients. Thus our objectives were to characterize skin cancer preventive counseling and clinical practices in a sample of pediatricians and identify correlates of these practices. Physicians practicing genera...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2003.03004.x

    authors: Gritz ER,Tripp MK,de Moor CA,Eicher SA,Mueller NH,Spedale JH

    更新日期:2003-01-01 00:00:00

  • Childhood granulomatous periorificial dermatitis with a good response to oral metronidazole.

    abstract::Childhood granulomatous periorificial dermatitis (CGPD) is a condition included in the spectrum of rosacea and perioral dermatitis that affects prepubescent children. It is characterized by papular eruptions located around the mouth, nose, and eyes that histopathologically show a granulomatous pattern. We report a 9-y...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12110

    authors: Rodriguez-Caruncho C,Bielsa I,Fernandez-Figueras MT,Ferrándiz C

    更新日期:2013-09-01 00:00:00

  • Eosinophilic pustular folliculitis of infancy suppressed with cetirizine.

    abstract::Eosinophilic pustular folliculitis of infancy is a rare inflammatory disease characterized by recurrent, itchy sterile pustules mainly located on the scalp. Topical agents are mostly effective to suppress the symptoms in the majority of cases. However, systemic agents that are safe for long-term use are required for p...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13764

    authors: Odyakmaz Demirsoy E,Demirsoy U,Ozod U,Kiran R

    更新日期:2019-05-01 00:00:00

  • Raynaud phenomenon after treatment of verruca vulgaris of the sole with intralesional injection of bleomycin.

    abstract::Intralesional injection of bleomycin (BLM) for the treatment of warts resistant to all conventional therapies is of certain interest because of the drug's low toxicity and its efficacy. However, delayed side effects may appear, particularly Raynaud phenomenon. Accordingly, some precautions must be taken in patients wi...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2001.018003249.x

    authors: Vanhooteghem O,Richert B,de la Brassinne M

    更新日期:2001-05-01 00:00:00

  • Macrocephaly-capillary malformation presenting with fetal arrhythmia.

    abstract::Macrocephaly-capillary malformation (OMIM 602501) is a rare overgrowth and asymmetry syndrome. Cardiac arrhythmias were reported to occur in few patients. We present a case in which fetal arrhythmia was the presenting symptom of the syndrome. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2011.01677.x

    authors: Kuint J,Globus O,Ben Simon GJ,Greenberger S

    更新日期:2012-05-01 00:00:00

  • Sacral hemangioma with sinus tract in an infant.

    abstract::Congenital midline cutaneous lesions should always alert the clinician to the possibility of spinal dysraphism. These lesions can take many different forms. The physician should be cognizant of such lesions in order to avoid potential neurologic complications. We present a patient with a midline sacral hemangioma asso...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1046/j.1525-1470.2003.20307.x

    authors: Winstanley D,Graham B,Blair M,Linfesty R,Tomita S,Matthews J

    更新日期:2003-05-01 00:00:00

  • Case report: vulvar lichen sclerosus in a premenarchal girl with a complicated biopsy.

    abstract::Lichen sclerosus is a T-lymphocyte mediated chronic cutaneous disorder with predilection for the vulva. In prepubertal girls, lichen sclerosus presents as vulvar discomfort, pruritus, bruising/bleeding, discharge, dysuria, or painful defecation. Diagnosis and treatment of lichen sclerosus is of utmost importance in th...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2009.00922.x

    authors: Yousefi M,Pride H,Elston D

    更新日期:2009-05-01 00:00:00

  • Giant condyloma acuminatum in an infant.

    abstract::We report a 10-month-old boy who presented with a giant perianal condyloma acuminatum, and a similar lesion on the neck. These lesions were treated by surgical excision with satisfactory results. This size, extent, and early age of appearance make this case highly unusual. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2009.00968.x

    authors: Tinsa F,Gharbi A,Essid A,Driss M,Bousnina S

    更新日期:2009-07-01 00:00:00

  • Bronchiolitis obliterans: a rare chronic pulmonary complication associated with Stevens-Johnson syndrome.

    abstract::Pulmonary manifestations are well recognized during the acute phase of Stevens-Johnson syndrome but persistent pulmonary sequela is rarely reported. We report two boys with bronchiolitis obliterans following the acute phase of Stevens-Johnson syndrome and discuss the clinical picture and treatment of persistent pulmon...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00433.x

    authors: Bakirtas A,Harmanci K,Toyran M,Razi CH,Turktas I

    更新日期:2007-07-01 00:00:00

  • Acquired port-wine stains in six pediatric patients.

    abstract:BACKGROUND/OBJECTIVES:Port-wine stains, also known as capillary malformations, are due to dermal vascular ectasia and dilation and are most commonly congenital; however, acquired port-wine stains (APWS) developing later in life have been noted in the literature, most commonly in the context of trauma. METHODS/RESULTS:...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.14019

    authors: Stephens MR,Putterman E,Yan AC,Castelo-Soccio L,Perman MJ

    更新日期:2020-01-01 00:00:00

  • A practical review of dermoscopy for pediatric dermatology part II: Vascular tumors, infections, and inflammatory dermatoses.

    abstract::In addition to the evaluation of melanocytic growths (Part I), dermoscopy is helpful in the identification and management of vascular tumors, skin infections, and inflammatory conditions. In this practical review, we present the classic dermoscopic findings of the following: vascular tumors, infectious conditions (mol...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.14284

    authors: Natsis NE,Gordon SC,Kaushik A,Seiverling EV

    更新日期:2020-09-01 00:00:00

  • Nodular lichen myxedematosus during childhood: a case report.

    abstract::Nodular lichen myxedematosus (LM) is a rare disease and is one of the five subtypes of localized LM. It is distinctly characterized by multiple nodules on the trunk and limbs with or without papular lesions. A healthy 6-year-old boy presented with complaints of "knots" on his right chest, upper limb, and thigh for 4 m...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12376

    authors: Zeng R,Li M,Jiang Y,Liu W

    更新日期:2014-11-01 00:00:00

  • Market trends in baby skin care products and implications for clinical practice.

    abstract::Although the U.S. pediatric skin care market is a $1.7 billion industry, little is known regarding the usage pattern of skin care products in very young children. We have begun to recognize that common over-the-counter skin care products may have positive or negative effects on skin barrier function. Thus, knowing wha...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12424

    authors: Gao X,Simpson EL

    更新日期:2014-11-01 00:00:00

  • Accessory tragus: Report of a case in a rare location on the nasal vestibule.

    abstract::A case of an accessory tragus located on the nasal vestibule is reported. This represents the third case of this entity located outside of a derivative of a branchial arch. All three of these cases were located in the nose/glabella region. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.14090

    authors: Moradi S,Castiglione C,Ehrig T

    更新日期:2020-03-01 00:00:00

  • Cervical occult spinal dysraphism: MRI findings and the value of a vascular birthmark.

    abstract::Spinal dysraphism is easily recognized in the overt form as a meningocele or myelomeningocele. The closed form or occult spinal dysraphism (OSD) can be overlooked. It occurs predominantly at the lumbosacral level, but OSD at the cervical level, although very rare, also occurs. The value of magnetic resonance imaging i...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.1995.tb00172.x

    authors: Enjolras O,Boukobza M,Jdid R

    更新日期:1995-09-01 00:00:00

  • Verruciform xanthoma in a patient with recessive dystrophic epidermolysis bullosa: Case report and literature review.

    abstract::Verruciform xanthoma (VX) is a rare finding thought to be caused by epidermal damage from trauma or inflammation and has been reported in a limited number of patients with recessive dystrophic epidermolysis bullosa (RDEB). Herein, we describe a 20-year-old woman with RDEB who developed a large, verrucous, pink plaque ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.14079

    authors: Stephens M,Rubin AI,Perman MJ

    更新日期:2020-03-01 00:00:00

  • Goodbye warts, hello vitiligo: Candida antigen-induced depigmentation.

    abstract::Depigmentation after the use of topical immune modulators is a rare but reported event. Herein we present what is to our knowledge the first case of vitiligo at a site of Candida antigen injection. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12049

    authors: Wilmer EN,Burkhart CN,Morrell DS

    更新日期:2013-11-01 00:00:00

  • Neonatal skin care: Developments in care to maintain neonatal barrier function and prevention of diaper dermatitis.

    abstract:BACKGROUND:Understanding the importance of the barrier function of the skin of preterm and term neonates is crucial in effective neonatal skin and diaper care. This literature search aimed to review the development of different practices in neonatal care to maintain skin barrier function, in turn preventing diaper derm...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/pde.13714

    authors: Burdall O,Willgress L,Goad N

    更新日期:2019-01-01 00:00:00

  • Allergic contact dermatitis to triethanolamine in a child.

    abstract::Triethanolamine is used as an emulsifier in many cosmetics and in topical medications, yet the occurrence of contact dermatitis to cosmetics containing triethanolamine is rare in childhood. Our case highlights how young age should not be a deterrent to investigation and demonstrates the importance of patch testing wit...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12537

    authors: Milanesi N,Berti S,Gola M

    更新日期:2015-05-01 00:00:00

  • Outpatient pediatric dermatologic surgery: experience in 296 patients.

    abstract::From January 2010 to December 2012, 296 skin biopsies were performed in pediatric patients using only local anesthesia (cream and infiltration). The biopsies were divided into three groups: biopsies of skin neoplasms, biopsies of skin rashes and biopsies of follicular-centered lesions. Our data demonstrate the possibi...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12414

    authors: D'Acunto C,Raone B,Neri I,Passarini B,Patrizi A

    更新日期:2015-05-01 00:00:00

  • Multiple milia in a newborn with congenital malformations: oral-facial-digital syndrome type 1.

    abstract::Oral-facial-digital syndrome type 1 (OMIM #311200) is an X-linked dominant, developmental disorder. Among the 13 described clinical variants of oral-facial-digital syndrome, oral-facial-digital syndrome type 1 is of significance to dermatologists due to presence of congenital milia and hypotrichosis, not described in ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2010.01334.x

    authors: Nanda A,Sharaf A,Alsaleh QA

    更新日期:2010-11-01 00:00:00

  • Follicular Mucinosis in a Male Adolescent with a History of Acute Myelogenous Leukemia and Graft-versus-Host Disease.

    abstract::Although many cases of follicular mucinosis are idiopathic, numerous others are associated with mycosis fungoides or, rarely, other neoplastic or inflammatory disorders. There are only three reported cases, all in adults, of follicular mucinosis arising in association with acute myelogenous leukemia, two of which invo...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.12724

    authors: Jefferson J,Taube J,Grossberg A

    更新日期:2016-01-01 00:00:00

  • Unnecessary milk elimination diets in children with atopic dermatitis.

    abstract::Milk elimination diets are frequently adopted in the treatment of atopic dermatitis, although the real prevalence of clinically relevant food allergy remains unclear and reports from different authors are often in disagreement. We investigated the percentage of children allergic to cow's milk compared with the rate of...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00323.x

    authors: Sinagra JL,Bordignon V,Ferraro C,Cristaudo A,Di Rocco M,Amorosi B,Capitanio B

    更新日期:2007-01-01 00:00:00

  • Familial Blau syndrome without uveitis caused by a novel mutation in the nucleotide-binding oligomerization domain-containing protein 2 gene with good response to infliximab.

    abstract::The proband in this study was a 4-year-old Mexican girl with Blau syndrome. She and her affected family members had skin rash and arthritis but no uveitis. Exome sequencing and DNA direct sequencing from blood samples revealed a novel nucleotide-binding oligomerization domain-containing protein 2 gene mutation in the ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13475

    authors: Toral-López J,González-Huerta LM,Martín-Del Campo M,Messina-Baas O,Cuevas-Covarrubias SA

    更新日期:2018-05-01 00:00:00

  • Sun exposure and protection practices in children after allogeneic hematopoietic stem cell transplantation: A Survey-Based Cross-Sectional Cohort Study.

    abstract:BACKGROUND/OBJECTIVE:Pediatric hematopoietic stem cell transplantation (HSCT) patients are at an increased risk for skin cancers. Sun exposure is a significant modifiable environmental risk factor. While patient education on sun protection and avoidance behaviors with regular dermatology evaluations are crucial for ped...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/pde.13984

    authors: Li EB,Song JS,Huang JT,Hawryluk EB,London WB,Guo D,Sridharan M,Fisher DE,Rea CJ,Lehmann LE,Duncan CN

    更新日期:2019-11-01 00:00:00

  • Morphea, diabetes mellitus type I, and celiac disease: case report and review of the literature.

    abstract::An 11-year-old girl with a history of diabetes mellitus type I and celiac disease presented with multiple, depressed patches of purple-brown skin on the right lower extremity and central back, with histopathologic features of early morphea. Though morphea may coexist with other autoimmune diseases, its presentation wi...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1525-1470.2009.00907.x

    authors: Firoz EF,Kamino H,Lehman TJ,Orlow SJ

    更新日期:2010-01-01 00:00:00

  • Chronic sole ulcer in a child with dyskeratosis congenita: An atypical wound successfully treated with punch grafting.

    abstract::Dyskeratosis congenita (DC) is an unusual inherited disease characterized by the triad of mucosal leukoplakia, nail dystrophy, and skin pigmentation. Hyperkeratosis of the palms and soles is another reported skin finding. This hyperkeratosis can lead to fissures, chronic erosion, and deep ulcerations. These atypical w...

    journal_title:Pediatric dermatology

    pub_type:

    doi:10.1111/pde.14316

    authors: Quintana-Castanedo L,Feito-Rodríguez M,Pérez-Conde I,Maseda-Pedrero R,Chiloeches-Fernández C,de Lucas Laguna R

    更新日期:2020-11-01 00:00:00

  • Severe neonatal congenital erythropoietic porphyria.

    abstract::Congenital erythropoietic porphyria is a rare form of porphyria, presenting during the neonatal period or during infancy. Clinical features include photosensitive blistering and severe anemia. Wood's lamp fluorescence of the diaper is a useful screening test. We describe a severely affected neonate with systemic invol...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2010.01376.x

    authors: Hogeling M,Nakano T,Dvorak CC,Maguiness S,Frieden IJ

    更新日期:2011-07-01 00:00:00